US7015285B2 - Composition and method for improving the adhesion of polyphenylene ether moldings to polyurethane foam - Google Patents
Composition and method for improving the adhesion of polyphenylene ether moldings to polyurethane foam Download PDFInfo
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- US7015285B2 US7015285B2 US10/325,724 US32572402A US7015285B2 US 7015285 B2 US7015285 B2 US 7015285B2 US 32572402 A US32572402 A US 32572402A US 7015285 B2 US7015285 B2 US 7015285B2
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- SNPOZKMCSJMKKV-UHFFFAOYSA-N COC1=C(C)C(C)=C(C)C(C)=C1C Chemical compound COC1=C(C)C(C)=C(C)C(C)=C1C SNPOZKMCSJMKKV-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/12—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/08—Polyethers derived from hydroxy compounds or from their metallic derivatives
- C08L71/10—Polyethers derived from hydroxy compounds or from their metallic derivatives from phenols
- C08L71/12—Polyphenylene oxides
- C08L71/123—Polyphenylene oxides not modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/905—Polyphenylene oxide
Definitions
- Polyphenylene ether resins generally show outstanding mechanical properties, thermal resistance, electrical characteristics, and flame resistance and are commonly used in a broad range of applications such as components in automobiles.
- various internal components in automobiles such as, e.g., instrument panels, arm rests, and top covers, require a high degree of thermal resistance making polyphenylene ether resin compositions ideally suited.
- Many of these same internal components are covered with a foamed polyurethane due to its desirable characteristics; however, polyphenylene ether resin compositions ordinarily have poor adhesion to foamed polyurethane.
- terpene phenol resin has been added compositions of polyphenylene ether resin and alkenyl aromatic resins; however, the adhesive properties of these compositions are still deficient.
- Various polar resins e.g., styrene-maleic anhydride copolymer have also been used in compositions of polyphenylene ether resin and alkenyl aromatic resins with limited success due to laminar peeling during molding and decreased mechanical properties.
- EP 0808871 discloses a resin composition of polyphenylene ether and polystyrene with enhanced adhesion and reduced laminar peeling from polyurethane brought about by the use of an ethylene-unsaturated carboxylic acid ester copolymer.
- EP 0808871 discloses a resin composition of polyphenylene ether and polystyrene with enhanced adhesion and reduced laminar peeling from polyurethane brought about by the use of an ethylene-unsaturated carboxylic acid ester copolymer.
- the present invention provides a composition having improved adhesion to polyurethane foam, said composition comprising at least one polyphenylene ether, at least one poly(alkenylaromatic) compound and at least one carboxylic acid containing copolymer derived from one or more olefins and one or more olefinic carboxylic acids.
- the composition may optionally further comprise at least one curing catalyst.
- the olefinic carboxylic acid residue in the copolymer is present from about 1 to 35 weight percent, preferably from about 5 to 25 weight percent.
- the carboxylic acid containing copolymer is present in an amount effective to provide adhesion of urethane foam to the composition.
- the composition is substantially free of ammonia-like odors.
- Another embodiment of the invention is to provide a method for improving the adhesion between a resinous thermoplastic substrate and a polyurethane foam wherein the method comprises blending at least one polyphenylene ether, at least one poly(alkenylaromatic) compound and at least one carboxylic acid containing copolymer derived from one or more olefins and one or more olefinic carboxylic acids, wherein the method optionally further comprising at least one curing catalyst.
- a thermoplastic article of manufacture that has enhanced adhesion to polyurethane foam and is useful as an automotive interior component such as an instrument panel.
- the principal components of the inventive composition that will yield a resinous thermoplastic substrate with enhanced adhesion to polyurethane foam are: a thermoplastic mixture or blend of at least one polyphenylene ether, at least one poly(alkenylaromatic) compound, at least one carboxylic acid containing copolymer and optionally, at least one curing catalyst.
- Other components can be present in the composition such as flame retardants, impact modifiers, mold releases, antioxidants, stabilizers, fillers, and mixtures thereof.
- polyphenylene ethers are known polymers comprising a plurality of structural units of the formula I: wherein in each of said units independently, each Q 1 is independently halogen, primary or secondary lower alkyl (i.e. alkyl containing up to seven carbon atoms), phenyl, haloalkyl, aminoalkyl, hydrocarbonoxy, or halohydrocarbonoxy, wherein at least two carbon atoms separate the halogen and the oxygen atoms; and each Q 2 is independently hydrogen, halogen, primary or secondary lower alkyl, phenyl, haloalkyl, hydrocarbonoxy or halohydrocarbonoxy as defined for Q 1 . Most often, each Q 1 is alkyl or phenyl, especially C 1-4 -alkyl, and each Q 2 is hydrogen.
- each Q 1 is independently halogen, primary or secondary lower alkyl (i.e. alkyl containing up to seven carbon atoms), phenyl, haloalkyl, aminoalkyl
- Both homopolymer and copolymer polyphenylene ethers are included.
- the preferred homopolymers are those containing 2,6-dimethyl-1,4-phenylene ether units.
- Suitable copolymers include random copolymers containing such units in combination with, for example, 2,3,6-trimethyl-1,4-phenylene ether units.
- polyphenylene ethers containing moieties prepared by grafting onto the polyphenylene ether in known manner such materials as vinyl monomers or polymers such as polystyrenes and elastomers, as well as coupled polyphenylene ethers in which coupling agents such as low molecular weight polycarbonates, quinones, heterocycles and formals, undergo reaction in known manner with the hydroxy groups of polyphenylene ether chains to produce a higher molecular weight polymer.
- the polyphenylene ether resins generally have a number average molecular weight in a range between about 3,000 and 40;000 in one embodiment of the present invention.
- the polyphenylene ether resins generally have an intrinsic viscosity (i.v.) in the range between about 0.15 and about 0.6 dl./g., as measured in chloroform at 25° C.
- the polyphenylene ethers may be typically prepared by the oxidative coupling of at least one monohydroxyaromatic compound such as 2,6-xylenol or 2,3,6-trimethylphenol using methods known in the art.
- Catalyst systems are generally employed for such coupling and they typically contain at least one heavy metal compound such as copper, manganese, or cobalt compound, usually in combination with various other materials.
- Particularly useful polyphenylene ethers for many purposes are those that comprise molecules having at least one aminoalkyl-containing end group.
- the aminoalkyl radical is typically located in an ortho position to the hydroxy group.
- Products containing such end groups may be obtained by incorporating an appropriate acid containing copolymer as one of the constituents of the oxidative coupling reaction mixture.
- 4-hydroxybiphenyl end groups typically obtained from reaction mixtures in which a by-product diphenoquinone is present.
- a substantial proportion of the polymer molecules, typically constituting as much as about 90% by weight of the polymer, may contain at least one of said aminoalkyl-containing and 4-hydroxybiphenyl end groups.
- polyphenylene ethers contemplated for use in the present invention include all those presently known, irrespective of variations in structural units or ancillary chemical features.
- the poly(alkenylaromatic) compounds employed in the thermoplastic resinous substrate composition include homopolymers and copolymers of such compounds as styrene, alpha.-methylstyrene, 4-methylstyrene and dibromostyrene.
- Polystyrene may be used in some embodiments.
- conventional rubber-modified polystyrenes sometimes designated “high impact polystyrene” or “HIPS” may be used.
- the polyphenylene ether may be present in amounts of at least about 20% by weight based on the weight of the two polymers, preferably between about 20 and 80% by weight based on the total weight of the polyphenylene ether and poly(alkenylaromatic) compound materials.
- the amount of polyphenylene ether in the polyphenylene ether-poly(alkylene aromatic) compound blend may be in a range between about 20% by weight and about 60% by weight based on the total weight of these two polymeric materials.
- the polyphenylene ether and poly(alkenylaromatic) compound mixture or blend may also contain conventional additives, especially flame retardant additives and impact modifiers.
- Flame retardant additives include brominated polystyrenes and phosphorus-containing chemicals such as triphenylphosphate, tri-t-butylphenylphosphate, tetraphenyl resorcinol bisphosphate, tetraxylyl resorcinol bisphosphate, tetraphenylhydroquinone bisphosphate and tetraxylyl hydroquinone bisphosphate.
- Impact modifiers for polyphenylene ether-poly(alkenylaromatic) compound mixtures or blends known in the art may also be employed. They include diblock and triblock copolymers of alkenylaromatic compounds such as styrene with aliphatic dienes such as butadiene and isoprene. The diene-derived blocks in said copolymers may be substantially saturated or may possess substantial unsaturation. One or more impact modifiers can be used. The composition may also include mold release compounds such as polyethylene.
- the carboxylic acid containing copolymer useful in the present invention is derived from one or more olefins and one or more olefinic carboxylic acids.
- Useful olefins include ethylene, propylene, 1-butene, 1,3-butadiene, isoprene, styrene, ⁇ -methyl styrene, and the like.
- Useful olefinic carboxylic acids include acrylic acid, methacrylic acid, fumaric acid and maleic acid.
- the olefinic carboxylic acid residue in the copolymer is present from about 1 to 35 weight percent, preferably from about 5 to 25 weight percent.
- Useful carboxylic acid containing copolymers are generally known in the art as are their methods of manufacture.
- the carboxylic acid containing copolymer is a styrene-acrylic acid copolymer, while in a second embodiment the carboxylic acid containing copolymer is a ethylene-acrylic acid copolymer and in a third embodiment, the carboxylic acid containing copolymer is a propylene-acrylic acid copolymer.
- the carboxylic acid containing copolymer is a polymerization product of monomers of a vinyl monomer selected from the group consisting of styrene, ethylene and propylene with a carboxylic acid containing monomer selected from acrylic acid and methacrylic acid, and combinations comprising various combinations of the foregoing monomers.
- the amount of carboxylic acid containing copolymer used in the compositions of the present invention can vary depending on the effectiveness of the particular copolymer to achieve the desired level of adhesion with the polyurethane foam.
- the level of carboxylic acid containing copolymer is within the range between about 1 weight percent and about 25 weight percent based on the combined weight of the polyphenylene ether and poly(alkenylaromatic) resins, more preferably within the range between about 7 weight percent and about 15 weight percent, and most preferably within the range between about 5 weight percent and about 10 weight percent all based on the combined weight of the polyphenylene ether and poly(alkenylaromatic) resins.
- the addition of more than one acid containing copolymer may further enhance the adhesion of polyurethane foam to the resinous thermoplastic substrate.
- the carboxylic acid containing copolymer may be a combination of styrene-acrylic acid copolymer and ethylene-acrylic-acid copolymer, while in a second embodiment a combination of ethylene-acrylic acid copolymer and propylene-acrylic acid copolymer may be used. In a third embodiment propylene-acrylic acid copolymer may be used in conjunction with styrene-acrylic acid copolymer.
- a phenolic additive may further enhance the adhesion of polyurethane foam to the resinous thermoplastic substrate.
- a second additive such as NirezTM 2150, which is a terpene phenol made from limonene and phenol, was found to increase the adhesive performance between the resinous thermoplastic substrate and the polyurethane foam.
- an optional addition ingredient for providing enhanced adhesion is a urethane catalyst.
- the urethane catalyst promotes reactions between the carboxylic acid containing copolymer and the polyurethane foam.
- urethane catalysts include organometallic compounds including, e.g., tin or potassium carboxylates.
- Other compounds may include organotins such as dibutyltin dilaurate, dibutyl tinoxide and dioctyl tinoxide.
- Bismuth and Zinc compounds may also used.
- the organotin catalyst is generally in a range between about 0.1% and about 10% by weight based upon the weight of the entire composition, preferably between about 0.5% and about 7% by weight, and more preferably, between about 3% and about 5% by weight.
- compositions of the present invention are prepared by mechanically blending the components in conventional mixing equipment, e.g., a single or twin screw extruder, Banbury mixer, or any other conventional melt compounding equipment.
- a vacuum may also be applied to during the compounding operation to further reduce odorous materials from the composition.
- the order in which the components of the composition are mixed is not generally critical and may be readily determined by one of skill in this art.
- the foam procedure that was used to formulate the resinous article with a foam polyurethane layer to be tested for adhesion follows: A very light coat of the food grade grease was applied with a paper towel to all interior surfaces of the foaming mold. The plaques tested (composition shown in Tables 1 and 2) were covered with a mesh screen and placed inside the mold. The mold contained 12 plaques at a time. The plaques were held on the bottom of the mold with a double-stick tape on their back surface. In a 1000 ml plastic disposable beaker, 382 grams of polyol Specflex NM815 (Dow Chemical) was weighed. In a separate 250 ml disposable beaker, 205 grams of polyisocyanate PAPI 95 (Dow Chemical) was added.
- the polyisocyanate was poured into the polyol beaker, and the contents were quickly mixed with overhead mechanical stirrer with a stirring speed of 5,000 rpm for 10 seconds.
- the homogeneous mixture was poured into the foaming mold immediately after mixing and a cover was placed on the mold, then it was fastened with four cover clamps. After about 20 minutes the foamed plaques were removed from the mold by taking the mold apart. The plaques with the polyurethane foam on the surface were then conditioned for 24 hours at room temperature. The samples were then cut into several 1 inch wide strips.
- the adhesion of the polyurethane foam to the plastic substrate covered with a mesh screen was accessed by pulling the foam apart from the substrate at 90 degree. The locus of failure, whether cohesive or adhesive was reported as noted in Table 2 and also discussed hereunder. ASTM D3359 procedure was used to rate the adhesion.
- Vancryl 65 Styrene-acrylic acid copolymer
- Primacor 59901 ethylene-acrylic acid copolymer
- Irganox 1010 was purchased from Ciba Specialty Chemicals.
- Cotin 100 and Fascat-4201 were bought from CasChem, Inc. and Atofina chemicals respectively while Hostastat HS-1 was obtained from Ciba Specialty Chemicals.
- PPE polyphenylene ether and (HIPS) high impact polystyrene were from General Electric Company.
- Plaque 1 represents the standard formulation and is used as the control model without any adhesion promoter additives.
- the control blend Plaque 1 contains only poly(2,6-dimethyl-1,4-phenylene oxide) (PPE) and HIPS (high impact polystyrene). This material had very poor polyurethane foam adhesion. The foam in Plaque 1 separated from the substrate adhesively.
- PPE poly(2,6-dimethyl-1,4-phenylene oxide)
- HIPS high impact polystyrene
- Plaque 2 had 40 parts by weight polyphenylene ether and 60 parts by weight HIPS plus 1 part by weight of Vancryl 65, which is a styrene-acrylic acid copolymer wherein the amount of acrylic acid is about 10 weight percent.
- the foam adhesion for Plaque 2 was significantly improved over Plaque 1. However, some adhesive failure in the polyurethane foam took place during the peel test.
- Plaque 3 had 40 parts by weight polyphenylene ether and 60 parts by weight HIPS plus 1 part by weight of Primacor 59901, which is ethylene acrylic acid copolymer wherein the amount of acrylic acid is about 20 weight percent.
- the foam adhesion for Plaque 3 was significantly improved over Plaque 1. However, some adhesive failure in the polyurethane foam took place during the peel test.
- Plaque 4 demonstrates the same composition as Plaque 2 except that about two (2) weight percent of Vancryl 65 is used in the PPE/HIPS formulation. Plaque 4 had excellent foam adhesion with the polyurethane foam. A complete cohesive failure occurred in the foam during the peel test on Plaque 4.
- Plaque 5 demonstrates the same composition as Plaque 4 except that instead of Vancryl 65 it has 2% of Primacor 59901. Plaque 5 had excellent foam adhesion with the polyurethane foam. A complete cohesive failure occurred in the foam during the peel test on Plaque 5.
- Plaque 6 demonstrates the same composition as Plaque 2 except that about 0.3 weight percent of Cotin 100, which is dibutyl tin oxide. Unexpectedly, it was discovered that just 0.3 weight percent of Cotin 100 significantly improved the foam adhesion performance.
- Plaque 7 demonstrates the same composition as Plaque 6 except that instead of Cotin 100, it uses 0.3% of Fascat 4201, which is an organotin urethane catalyst. As noted by these data, as little as 0.3 percent of Fascat 4201 significantly improved the foam adhesion performance (5). A complete cohesive failure occurred in the polyurethane foam during the peel test on Plaque 7.
- Plaque 4 was made using a combination of acid-containing materials and terpene phenolic resin additives to improve the urethane foam adhesion.
- the composition of the improved formulation are shown in Table 2.
- the formulation shown in Plaque 8 was made employing both Nirez 2150, terpene phenol made by reacting limonene and phenol, Primacor 59901, and Cotin 100.
- the foam adhesion test that was conducted was similar to that of Example 1. The foam adhesion between the resinous substrate and the polyurethane foam was good.
- the enhancement in adhesion achieved by using the resin with carboxylic acid containing copolymer is significant especially in conjunction with catalyst. Additionally, the compositions of the present invention exhibit reduced ammonia-like odors associated with amines that were previously used for improving adhesion.
- thermoplastic articles of manufacture such as those used as an automotive instrument panel comprising thermoplastic substrate and polyurethane foam, exhibiting good adhesion between the polyurethane foam and the substrate material by way of a simple and cost effective process and also avoiding the problems of ammonia-like bad odor.
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Abstract
Description
wherein in each of said units independently, each Q1 is independently halogen, primary or secondary lower alkyl (i.e. alkyl containing up to seven carbon atoms), phenyl, haloalkyl, aminoalkyl, hydrocarbonoxy, or halohydrocarbonoxy, wherein at least two carbon atoms separate the halogen and the oxygen atoms; and each Q2 is independently hydrogen, halogen, primary or secondary lower alkyl, phenyl, haloalkyl, hydrocarbonoxy or halohydrocarbonoxy as defined for Q1. Most often, each Q1 is alkyl or phenyl, especially C1-4-alkyl, and each Q2 is hydrogen.
TABLE 1 | |||||||
Composition | Plaque 1 | Plaque 2 | Plaque 3 | Plaque 4 | Plaque 5 | Plaque 6 | Plaque 7 |
PPE | 40 | 40 | 40 | 40 | 40 | 40 | 40 |
HIPS | 60 | 60 | 60 | 60 | 60 | 60 | 60 |
Vancryl 65 | 1 | 2 | 1 | 1 | |||
Primacor | 1 | 2 | |||||
5990l | |||||||
Cotin 100 | 0.3 | ||||||
Fascat 4201 | 0.3 | ||||||
Foam | (1)No | (3)Marginal | (3)Marginal | (5)Good | (5)Good | (5)Good | (5)Good |
Adhesion | adhesion | adhesion | adhesion | adhesion | adhesion | adhesion | adhesion |
TABLE 2 | |||
Ingredient | Plaque 8 | ||
PPE (0.40 intrinsic viscosity) | 36 | ||
HIPS | 47 | ||
Kraton G1651 (SEBS rubber) | 4 | ||
Kraton D1101: Styrene-butadiene-Styrene | 4 | ||
unsaturated rubber | |||
Hostastat HS-1 | 1.5 | ||
Primacor 5990I | 1.5 | ||
Ethylene-acrylic acid copolymer | |||
Cotin 100 (urethane catalyst) | 0.2 | ||
ZnO/ZnS | 0.1/0.1 | ||
Irganox 1010 | 0.2 | ||
(antioxidant) | |||
Foam adhesion | Good | ||
Claims (20)
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US9683071B2 (en) | 2012-12-21 | 2017-06-20 | Basf Se | Rigid polyurethane foam |
CN104816423A (en) * | 2015-04-14 | 2015-08-05 | 长春富维—江森自控汽车饰件系统有限公司 | Forming method of automobile instrument panel |
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